TY - JOUR
T1 - Acoustic prepulse inhibition in male and female prairie voles
T2 - Implications for models of neuropsychiatric illness
AU - Jones, Carolyn E.
AU - Navis, Tom M.
AU - Teutsch, Peyton
AU - Opel, Ryan A.
AU - Lim, Miranda M.
N1 - Funding Information:
This work was supported by VA Biomedical Laboratory Research & Development (BLR&D) Career Development Award (CDA) # IK2 BX002712, Portland VA Research Foundation, Brain & Behavior Foundation NARSAD Award, Collins Medical Trust, and NIH EXITO Institutional Core, #UL1GM118964 to MML; NIH T32 5T32AA007468-29 and NIH T32 5T32HL083808-10 to CEJ; and NIH T32 5T32AA007468-32 to TMN.
Publisher Copyright:
© 2018
PY - 2019/3/15
Y1 - 2019/3/15
N2 - Sensory gating, the ability to suppress sensory information of irrelevant stimuli, is affected in several neuropsychiatric diseases, notably schizophrenia and autism. It is currently unclear how these deficits interact with other hallmark symptoms of these disorders, such as social withdrawal and difficulty with interpersonal relationships. The highly affiliative prairie vole (Microtus ochrogaster) may be an ideal model organism to study the neurobiology underlying social behavior. In this study, we assessed unimodal acoustic sensory gating in male and female prairie voles using the prepulse inhibition (PPI) paradigm, whereby a lower amplitude sound (prepulse) decreases the startle response to a high amplitude sound (pulse) compared to the high amplitude sound alone. Prairie voles showed evidence of PPI at all prepulse levels compared to pulse alone, with both males and females showing similar levels of inhibition. However, unlike what has been reported in other rodent species, prairie voles did not show a within-session decrease in startle response to the pulse alone, nor did they show a decrease in startle response to the pulse over multiple days, highlighting their inability to habituate to startling stimuli (short- and long-term). When contrasted with a cohort of male wildtype C57Bl/6J mice that underwent a comparable PPI protocol, individual voles showed significantly higher trial-by-trial variability as well as longer latency to startle than mice. The benefits and caveats to using prairie voles in future sensory gating experiments are discussed.
AB - Sensory gating, the ability to suppress sensory information of irrelevant stimuli, is affected in several neuropsychiatric diseases, notably schizophrenia and autism. It is currently unclear how these deficits interact with other hallmark symptoms of these disorders, such as social withdrawal and difficulty with interpersonal relationships. The highly affiliative prairie vole (Microtus ochrogaster) may be an ideal model organism to study the neurobiology underlying social behavior. In this study, we assessed unimodal acoustic sensory gating in male and female prairie voles using the prepulse inhibition (PPI) paradigm, whereby a lower amplitude sound (prepulse) decreases the startle response to a high amplitude sound (pulse) compared to the high amplitude sound alone. Prairie voles showed evidence of PPI at all prepulse levels compared to pulse alone, with both males and females showing similar levels of inhibition. However, unlike what has been reported in other rodent species, prairie voles did not show a within-session decrease in startle response to the pulse alone, nor did they show a decrease in startle response to the pulse over multiple days, highlighting their inability to habituate to startling stimuli (short- and long-term). When contrasted with a cohort of male wildtype C57Bl/6J mice that underwent a comparable PPI protocol, individual voles showed significantly higher trial-by-trial variability as well as longer latency to startle than mice. The benefits and caveats to using prairie voles in future sensory gating experiments are discussed.
KW - Acoustic startle
KW - Autism
KW - Comparative neuroscience
KW - Habituation
KW - Schizophrenia
KW - Sensory gating
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U2 - 10.1016/j.bbr.2018.12.022
DO - 10.1016/j.bbr.2018.12.022
M3 - Article
C2 - 30550951
AN - SCOPUS:85058657999
SN - 0166-4328
VL - 360
SP - 298
EP - 302
JO - Behavioural Brain Research
JF - Behavioural Brain Research
ER -